Passer au contenu principal
Rechercher

Associate Director, Cell Therapy Learning Lead

Lieu Varsovie, Voïvodie de Mazovie, Pologne Job ID R-249855 Date de publication 04/10/2026

TheAssociateDirector,Cell TherapyLearning Lead(ADCTLL)rolewill work in a collaborative manner with other members of theCell Therapy Clinical Operations(CTCO)Business Processes, Quality & Learning(BPQL)team.

This roleis responsible tobothoversee and lead thedevelopmentoflearning materialsfor Cell Therapy-specificprocedures as well as tosupport thedelivery Clinical Execution Excellence, ensuring an effective end-to-end delivery of clinical trials.

TheAD CT LLrole will functionto supportteams across CTCOin order toensure that all CTCO trials areprepared forbothinternal and external auditsand inspections.

TheAD CT LLrole has a specific area of expertise within CTCO BPQL in the following manner:

  • Work closelywith CTCO Process Ownersin order toensure that any established processes adhereto AZ global quality standards.

  • Deliver or drive the developmentofquality-relatedinitiatives andcontinuousimprovement programmesthat would support improved Quality andCompliancewithinCTCO trialsand within CTCO-related processes and initiatives.

  • FirstlineofQuality support toallCTCO trialsand CTCO-related initiatives.

  • Tooperatewithin established AstraZenecanetworks, including but not limited to Process Quality,Learning & Transformation(PQLT).

Typical responsibilities:

Learning Materials Development

  • Lead and manage the deliveryof assigned learningobjectivesandpriorities for CTCO

  • Ensuring thatexisting and updated materials meet AZs requirementsregardingprocess clarity, 

CTCTLLworkscloselywith the BPQL team,ensuring:

  • Insights related to CTCO-specificprocess-relatedissues requiring corrective actions are documented for potential future process improvements.

  • Process KPIs & measurement:Support development,using quality-related datatoinform process and business improvement activities.

  • Performeffectiveness checks as neededtosupport the remediation of study-related CAPAs and if needed toverify theuptake and adoption of new and changedCTCO-relatedprocesses.

Escalate, as needed,to2ndLine Quality and the broader CTQNany issues or risksrelated to anyCTCO-related studies or initiatives

Communicate on a routine basis, relevant quality-relatedinsightsand feedback to the greater CTCO organization

Requirements:

Essential

  • Bachelor of Science inan appropriate disciplineor equivalent experience

  • At least7yearsofrelevantoperationaland/or qualityexperience in Drug Development within a pharmaceutical or clinical background

  • Strong knowledgeof business process, technology and ClinicalStudy information knowledge

  • Demonstratedtimemanagementacumenand proven skills to deliverresponses andsupport

  • Experience in working successfully and collaboratively withboth internal andexternal partners 

  • Demonstratedstrongwritten and verbal communication and influencing skills, negotiation, collaboration, problem solving, presentation, knowledge transfer (mentoring), conflictmanagementand interpersonal skills

  • Strongknowledge of Clinical Trials related international regulations,guidelinesand standards(ICH GCP, FDA, EMAregulationsand guidelines as minimum), as well as AZ internal standards and procedures, across functions 

  • Ability to effectively influence and communicate; ability to engage and collaborate across boundaries with problem solving focus

  • Ability to manage multiple competing priorities,demonstratinga growth mindset,innovation,ownershipand accountability

Desirable

  • Strongreputationwithin the business and industry

  • Strong understanding and knowledgeregardingCell Therapy-relevant procedures

  • Experience ofutilizingstandard process improvement methodologies (e.g. Lean Six Sigma) toidentifyroot causes of process issues andidentifyareas of process improvement

  • Experience in the development and management of Business Process to deliver business performance

Date Posted

10-kwi-2026

Closing Date

30-kwi-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.



AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Rejoignez notre réseau de talents

Inscrivez-vous pour recevoir des alertes emplois AstraZeneca.

S'inscrire
Glassdoor logo Rated four stars on Glassdoor

Une culture d'entreprise inspirante, des missions riches, des managers qui accompagnent et soutiennent. Des opportunités de rotation rapide au sein de l'entreprise. Ils accordent de l'importance à l'inclusion et à la diversité.